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HRID 1715445作成日:2026年10月26日

Ammonium Chloride → 6-[2-(2,6-Dichloro-4-methyl-phenoxy)-ethoxy]-5',6'-dihydro-2'H-[3,4']bipyridinyl-1',3'-dicarboxylic acid 1'-tert-butyl ester 3'-methyl ester

https://huagongshe.com/reaction/1715445

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物1-Tert-butyl 3-methyl 4-(trifluoromethanesulfonyloxy)-1,2,5,6-tetrahydropyridine-1,3-dicarboxylateHCID 15221936—
反応物5-Bromo-2-(2-(2,6-dichloro-4-methylphenoxy)ethoxy)pyridineHCID 44816668—
反応物ButyllithiumHCID 178418339—
触媒ZincchlorideHCID 3007855—
触媒HCID 178418397HCID 178418397—
溶媒TetrahydrofuranHCID 8028—
生成物6-[2-(2,6-Dichloro-4-methyl-phenoxy)-ethoxy]-5',6'-dihydro-2'H-[3,4']bipyridinyl-1',3'-dicarboxylic acid 1'-tert-butyl ester 3'-methyl esterHCID 6714906670.4%

反応条件

温度-78 °C

反応手順

BuLi (1.6M in hexane, 39.3 mL, 45.2 mmol) was added to a sol. of 5-bromo-2-[2-(2,6-dichloro-4-methyl-phenoxy)-ethoxy]-pyridine (13.0 g, 34.5 mmol) in THF (700 mL) at −78° C. The mixture was stirred for 1 h at −78° C., and ZnCl2 (0.72M in THF, 78.6 mL, 56.5 mmol) was added. The mixture was allowed to warm up to rt. 4-Trifluoromethanesulfonyloxy-5,6-dihydro-2H-pyridine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester (WO 2004/002957, 11.0 g, 28.3 mmol) and Pd(PPh3)4 (813 mg, 0.704 mmol) were added. The mixture was stirred for 30 min at 70° C., then overnight at rt. Aq. sat. NH4Cl was added, and the mixture was extracted with EtOAc (2×). The org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of the crude by FC (heptane/EtOAc 9:1→5:5) yielded the title compound (10.7 g, 70%). LC-MS: tR=1.16 min; ES+: 537.33.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07799805B2
出典データセットuspto-grants-2010_09
ORD IDord-1378380a336e4fcc917a0ef6d6c31942
出典メモuspto-grants-2010_09